Canonical Allele Identifier:
CA337100558
Gene:
Linked Data
ClinVar Variation Id:
690213
ClinVar RCV Id:
RCV000851105
dbSNP Id:
rs199833246
MyVariant Identifiers:
chrMT:g.15889T>C (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.15889T>C , J01415.2:m.15889T>C | GRCh38 |